Precia Group
Clinical research organization and site management organization focused on increasing representation of women and underrepresented populations in clinical trials. Offers clinical operations, study design, site network development, data management, regulatory strategy, and biobanking support with an emphasis on community-based research and equitable access.
Industries
Nr. of Employees
small (1-50)
Products
Women's Health Clinical Research Services
Comprehensive clinical research and CRO services focused on women's health, addressing gender bias and promoting inclusivity in clinical trials across all phases.
KOL Access, Engagement and Facilitation
Access to a vast network of women's health experts who consult in study design, standard of care, and market readiness.
Consulting
Consulting on FDA Guidance Inclusion Plans and advising community hospital systems establishing biobanks and research institutes.
Biobanking
Partnership with industry leading biospecimen storage solutions to meet short- and long-term banking needs.
Site Selection
Identify appropriate principal investigators and match sponsor needs with the patient pool through feasibility assessments.
Study Design
Study design consulting ensuring scientific integrity and protocol and specimen SOP development.
Women's Health Clinical Research Services
Comprehensive clinical research and CRO services focused on women's health, addressing gender bias and promoting inclusivity in clinical trials across all phases.
KOL Access, Engagement and Facilitation
Access to a vast network of women's health experts who consult in study design, standard of care, and market readiness.
Consulting
Consulting on FDA Guidance Inclusion Plans and advising community hospital systems establishing biobanks and research institutes.
Biobanking
Partnership with industry leading biospecimen storage solutions to meet short- and long-term banking needs.
Site Selection
Identify appropriate principal investigators and match sponsor needs with the patient pool through feasibility assessments.
Study Design
Study design consulting ensuring scientific integrity and protocol and specimen SOP development.
Services
Feasibility assessments, pre-site visits, patient-pool matching, and principal investigator identification to support site selection.
Protocol and specimen SOP development designed to integrate with clinical workflows while maintaining scientific integrity.
Expedited contracting with network sites, IRB coordination, site initiation visits, and development of customized data structures for study readiness.
Performance management tools and staffing strategies to optimize recruitment and site performance metrics.
Medical record abstraction processes to enable timely access to comprehensive participant clinical data across care teams.
Partnerships with biospecimen storage providers to meet short- and long-term specimen banking requirements and support cohort studies.
Feasibility assessments, pre-site visits, patient-pool matching, and principal investigator identification to support site selection.
Protocol and specimen SOP development designed to integrate with clinical workflows while maintaining scientific integrity.
Expedited contracting with network sites, IRB coordination, site initiation visits, and development of customized data structures for study readiness.
Performance management tools and staffing strategies to optimize recruitment and site performance metrics.
Medical record abstraction processes to enable timely access to comprehensive participant clinical data across care teams.
Partnerships with biospecimen storage providers to meet short- and long-term specimen banking requirements and support cohort studies.
Expertise Areas
- Clinical trial management
- Site management and network development (SMO)
- Women’s health and maternal-perinatal research
- Community-based research
Key Technologies
- Electronic data capture (EDC)
- Medical record abstraction and EHR data integration
- Biobanking and specimen storage systems
- Multi-omics sample harmonization
News & Updates
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